Balancing Autonomy and Protection: Ohio Considers Supported Decision-Making Legislation for Adults with Developmental Disabilities

For adults with developmental disabilities in Ohio, navigating the transition into adulthood and the myriad choices that accompany it has long presented a binary and often rigid legal dilemma. Historically, families and individuals faced a stark ultimatum: either retain full, unassisted legal control over all life decisions, or subject the individual to a probate court proceeding that could declare them legally incompetent and install a guardian with sweeping authority over their daily lives.
Now, a legislative measure winding its way through the Ohio General Assembly aims to construct a vital middle ground. Senate Bill 35, a bipartisan proposal designed to formally recognize "supported decision-making," seeks to provide a legal framework through which adults with developmental disabilities can enlist trusted advisors to help them process information, weigh alternatives, and articulate their choices—all without surrendering their fundamental right to make the ultimate decision.
While the bill sailed through the Ohio Senate with a unanimous vote last year, its current examination by the House Children and Human Services Committee has illuminated a complex policy debate. At the heart of the discourse lies a delicate balancing act: how to empower individuals with greater independence and dignity while simultaneously establishing adequate safeguards to prevent exploitation and undue influence in an arrangement that operates largely outside the direct oversight of the judicial system.
Legislative Mechanics and the Framework of SB 35
Supported decision-making is not an entirely novel concept in Ohio. For generations, adults with developmental disabilities have informally relied on parents, siblings, close friends, and specialized professionals for advice when managing their finances, healthcare, and living arrangements. However, these informal networks lack official recognition, often leaving institutions such as banks, hospitals, and housing authorities hesitant or legally unable to share information with advisors or recognize their collaborative role.
Senate Bill 35, sponsored by Republican Senators Jerry Cirino of Kirtland and Michele Reynolds of Canal Winchester, seeks to codify this practice. Under the current draft of the legislation, the legal presumption remains that all adults with developmental disabilities are competent unless a court of law determines otherwise.
Should an adult who is deemed of sound mind voluntarily choose to enter into a supported decision-making arrangement, the agreement must be formalized in writing. The plan requires the informed consent of the principal—the individual with the disability—and must be executed before a notary public or signed by two independent adult witnesses who are not parties to the agreement.
The duties assigned to a designated supporter under the bill are consultative rather than authoritative. Supporters are authorized to help explain complex options and potential consequences, assist in communicating decisions, help gather relevant medical, educational, or financial information, and participate in discussions with third parties on the principal’s behalf. Crucially, the adult retaining the supporter dictates the boundaries of the arrangement, maintaining the legal authority to act independently and retaining the absolute power to modify or terminate the agreement at any time simply by notifying the supporter.
Furthermore, the legislation establishes that supporters operate under a fiduciary duty, meaning they are legally bound to prioritize the principal’s best interests over their own. A supporter who breaches this obligation can be held civilly liable for any resulting damages. To assist families, professionals, and individuals, the Ohio Department of Developmental Disabilities would be mandated to develop a standardized model plan and comprehensive educational materials.
The Push for Alternatives to Guardianship
Proponents of Senate Bill 35 frame the legislation as a necessary and less restrictive alternative to traditional guardianship. In Ohio, guardianship is established through county probate courts following a judicial finding that an individual is incapable of managing their personal affairs. Once appointed, a guardian assumes control over specific aspects of the ward’s life, a process that disability advocates argue can inadvertently strip individuals of their civil liberties and personal autonomy.
During recent committee hearings, sponsors and advocates emphasized the psychological and developmental benefits of fostering self-determination. "We don’t always need to approach everything from a guardian or a control standpoint," Sen. Reynolds told her House colleagues. "We need to coach individuals to be able to self-actualize and live to their fullest potential."
This philosophy resonates deeply with families navigating the state’s social services and legal systems. Derek Graham, an Ohio attorney and father of a daughter with Down syndrome, testified before lawmakers regarding the immediate societal pressure families face as their children reach the age of majority. Graham recounted how individuals who had never met his daughter casually assumed she would automatically require a guardian upon turning 18.
"My wife and I, we don’t want to make decisions for our daughter," Graham told the committee. "I want to continue to make decisions with her."
Scott Lundregan, representing ElevateDD, echoed this sentiment, arguing that traditional estate planning and guardianship paradigms are inherently deficit-based. "Virtually everything with estate planning and guardianship is all focused on what these people can’t do," Lundregan said. "Supported decision-making is about what they can do."
Real-world applications of these principles already exist. Stephanie Leppert, an Ohio resident with Down syndrome, shared her personal experience of utilizing a collaborative network of family, friends, and service coordinators. With their advice and backing, Leppert successfully moved out of her parents’ home after living there for 37 years and has since maintained an independent lifestyle.
Ohio’s legislative push aligns with a broader national trend. According to data compiled by I Decide Kansas, a disability rights advocacy resource, at least 25 states and the District of Columbia have already enacted legislation recognizing supported decision-making agreements as legally valid instruments.
Safeguards, Oversight, and Concerns from the Legal Community
Despite widespread enthusiasm from disability rights advocates and families, Senate Bill 35 has drawn rigorous scrutiny from legal professionals, magistrates, and protective service organizations who worry about potential vulnerabilities. Because supported decision-making agreements are established privately rather than filed and monitored through probate courts, critics point to a lack of institutional oversight.
Chief Magistrate Lisa Wiseman of the Montgomery County Probate Court testified before the House committee to clarify the judiciary’s limited role under the proposed statute. Unlike a formal guardianship, where courts periodically review reports and monitor the ward’s well-being, a supported decision-making agreement operates outside the courtroom. "The court would not be involved, typically, unless somebody has brought an action to the court," Wiseman explained, noting that estranged family members or protective agencies might remain entirely unaware that an agreement is even in effect.
This decentralized nature raises urgent questions regarding how to detect and intercept coercion, undue influence, or financial exploitation before irreversible harm occurs. While the bill requires the principal to sign the agreement voluntarily before a notary or witnesses, no neutral judicial officer evaluates the individual’s comprehension or vulnerability at the outset.
Legal scholars and practitioners have zeroed in on specific ambiguities within the legislative text. The current draft stipulates that an adult with a developmental disability who is "of sound mind" may voluntarily enter into a plan. However, critics argue the language is imprecise and fails to establish a clear, standardized threshold for determining capacity, nor does it specify who is responsible for making that assessment.
Attorney Caroline A. Lahrmann, a co-guardian for two adults with developmental disabilities, offered some of the most critical testimony during the hearings. Lahrmann took issue with the statutory wording, arguing that it does not explicitly mandate that an individual be of sound mind prior to execution, potentially exposing vulnerable adults to legally binding arrangements they are incapable of fully comprehending. Characterizing aspects of the draft as legally loose, Lahrmann contended that the framework treats individuals with developmental disabilities with less procedural caution than other Ohioans.
"This bill treats people with developmental disabilities with less care than any other Ohioan," Lahrmann warned lawmakers, adding that the proposal lacks mandatory-reporting requirements for third parties who suspect abuse and fails to categorically exclude individuals with criminal backgrounds or paid service providers from serving as supporters.
In contrast, Kristen Henry of Advocacy and Protective Services defended the bill’s structural integrity. Henry noted that the phrase "of sound mind" mirrors established standards already successfully utilized in other areas of Ohio jurisprudence, such as the creation of healthcare powers of attorney. Furthermore, Henry argued that existing professional ethics and statutory mandates within Ohio’s developmental disability infrastructure already compel most service professionals to report suspected abuse, neglect, or exploitation regardless of whether a formal decision-making agreement is present.
Lingering Gray Areas and the Road Ahead
As the legislation continues its progression through the House Children and Human Services Committee, lawmakers and stakeholders are grappling with several unresolved gray areas:
- Capacity Standards: Uncertainty remains over how and by whom the "sound mind" threshold will be evaluated before an agreement is executed.
- Voluntariness and Coercion Detection: With no mandatory court approval process, committee leaders, including Chair Andrea White and Rep. Tracy Richardson, have questioned how manipulation occurring outside formal observation will be caught.
- Supporter Qualifications: The current absence of mandatory background checks or exclusions for paid providers leaves enforcement reliant primarily on post-hoc fiduciary liability and conflict-of-interest disclosures.
- Interplay with Existing Guardianships: The bill does not explicitly detail how a supported decision-making plan would function if superimposed upon an existing limited guardianship, leaving courts to default to the guardian as the ultimate authority.
- Termination Tracking: Because plans can be dissolved by simple notification, third-party institutions such as banks and medical facilities lack a centralized registry to verify whether an active agreement has been modified or revoked.
Whether Senate Bill 35 can successfully thread the needle between expanding personal freedom and maintaining robust protective oversight will depend heavily on potential amendments considered by the House. For thousands of Ohioans with developmental disabilities and their aging parents, the outcome of this legislative debate carries profound implications for how autonomy, trust, and protection are legally defined in the decades to come.







